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Cell Reactant:Reverse transcriptase (HIV-1 RT)(1-350)
Syringe Reactant:BDBM2483
Meas. Tech.:Enzyme Inhibition
Entry Date:06/16/17
 
ΔG°:-158±47.7 (kJ/mole)
pH:n/a
Log10Kb:n/a
Temperature:298.15±0 (K)
ΔH° :-240± (kJ/mole)
ΔHobs:n/a
Ionic Strength:n/a
Corrected for ΔHioniz:n/a
Protons Released:n/a
ΔCp :n/a
Stoich. Param.:n/a
ΔS° : -0.277±0.156 (kJ/mole-K)
Comments:n/a
 
Citation Decha PIntharathep PUdommaneethanakit TSompornpisut PHannongbua SWolschann PParasuk V Theoretical studies on the molecular basis of HIV-1RT/NNRTIs interactions. J Enzyme Inhib Med Chem 26:29-36 (2011) [PubMed]
More Info.:  Get all data from this article ,  ITC RUN data
 
Reverse transcriptase (HIV-1 RT)(1-350)
Source:n/a
Purity:n/a
Prep. Method:n/a
Name:Reverse transcriptase (HIV-1 RT)(1-350)
Synonyms:n/a
Type:Enzyme
Mol. Mass.:39217.95
Organism:Human immunodeficiency virus type 1
Description:HIV-1 RT variant (1-350 aa)
Residue:350
Sequence:
MGARASVLSGGELDRWEKIRLRPGGKKKYKLKHIVWASRELERFAVNPGLLETSEGCRQI
LGQLQPSLQTGSEELRSLYNTVATLYCVHQRIEIKDTKEALDKIEEEQNKSKKKAQQAAA
DTGHSNQVSQNYPIVQNIQGQMVHQAISPRTLNAWVKVVEEKAFSPEVIPMFSALSEGAT
PQDLNTMLNTVGGHQAAMQMLKETINEEAAEWDRVHPVHAGPIAPGQMREPRGSDIAGTT
STLQEQIGWMTNNPPIPVGEIYKRWIILGLNKIVRMYSPTSILDIRQGPKEPFRDYVDRF
YKTLRAEQASQEVKNWMTETLLVQNANPDCKTILKALGPAATLEEMMTAC
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM2483
Source:n/a
Purity:n/a
Prep. Method:n/a
NameBDBM2483
Synonyms:(4S)-6-chloro-4-(2-cyclopropylethynyl)-4-(trifluoromethyl)-2,4-dihydro-1H-3,1-benzoxazin-2-one | CHEMBL223228 | DMP-266 | EFV | Efavirenz | Efavirenz (EFV) | L-743,726 | Sustiva
TypeSmall organic molecule
Emp. Form.C14H9ClF3NO2
Mol. Mass.315.675
SMILESFC(F)(F)[C@]1(OC(=O)Nc2ccc(Cl)cc12)C#CC1CC1 |r|
Structure
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